Pseudohypoaldosteronism Type II Caused by Mutation Presented with Visual Impairment.
- Author:
Qiao WANG
1
;
Bing-Yan CAO
1
;
Chang SU
1
;
Wen-Jing LI
1
;
Chun-Xiu GONG
1
Author Information
- Publication Type:Letter
- MeSH: Cullin Proteins; genetics; Humans; Mutation; Protein-Serine-Threonine Kinases; Pseudohypoaldosteronism; genetics; Vision Disorders; genetics
- From: Chinese Medical Journal 2018;131(15):1879-1881
- CountryChina
- Language:English
